A novel deep learning-based point-of-care diagnostic method for detecting Plasmodium falciparum with fluorescence digital microscopy.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 11 08 2020
accepted: 30 10 2020
entrez: 17 11 2020
pubmed: 18 11 2020
medline: 5 1 2021
Statut: epublish

Résumé

Malaria remains a major global health problem with a need for improved field-usable diagnostic tests. We have developed a portable, low-cost digital microscope scanner, capable of both brightfield and fluorescence imaging. Here, we used the instrument to digitize blood smears, and applied deep learning (DL) algorithms to detect Plasmodium falciparum parasites. Thin blood smears (n = 125) were collected from patients with microscopy-confirmed P. falciparum infections in rural Tanzania, prior to and after initiation of artemisinin-based combination therapy. The samples were stained using the 4',6-diamidino-2-phenylindole fluorogen and digitized using the prototype microscope scanner. Two DL algorithms were trained to detect malaria parasites in the samples, and results compared to the visual assessment of both the digitized samples, and the Giemsa-stained thick smears. Detection of P. falciparum parasites in the digitized thin blood smears was possible both by visual assessment and by DL-based analysis with a strong correlation in results (r = 0.99, p < 0.01). A moderately strong correlation was observed between the DL-based thin smear analysis and the visual thick smear-analysis (r = 0.74, p < 0.01). Low levels of parasites were detected by DL-based analysis on day three following treatment initiation, but a small number of fluorescent signals were detected also in microscopy-negative samples. Quantification of P. falciparum parasites in DAPI-stained thin smears is feasible using DL-supported, point-of-care digital microscopy, with a high correlation to visual assessment of samples. Fluorescent signals from artefacts in samples with low infection levels represented the main challenge for the digital analysis, thus highlighting the importance of minimizing sample contaminations. The proposed method could support malaria diagnostics and monitoring of treatment response through automated quantification of parasitaemia and is likely to be applicable also for diagnostics of other Plasmodium species and other infectious diseases.

Sections du résumé

BACKGROUND
Malaria remains a major global health problem with a need for improved field-usable diagnostic tests. We have developed a portable, low-cost digital microscope scanner, capable of both brightfield and fluorescence imaging. Here, we used the instrument to digitize blood smears, and applied deep learning (DL) algorithms to detect Plasmodium falciparum parasites.
METHODS
Thin blood smears (n = 125) were collected from patients with microscopy-confirmed P. falciparum infections in rural Tanzania, prior to and after initiation of artemisinin-based combination therapy. The samples were stained using the 4',6-diamidino-2-phenylindole fluorogen and digitized using the prototype microscope scanner. Two DL algorithms were trained to detect malaria parasites in the samples, and results compared to the visual assessment of both the digitized samples, and the Giemsa-stained thick smears.
RESULTS
Detection of P. falciparum parasites in the digitized thin blood smears was possible both by visual assessment and by DL-based analysis with a strong correlation in results (r = 0.99, p < 0.01). A moderately strong correlation was observed between the DL-based thin smear analysis and the visual thick smear-analysis (r = 0.74, p < 0.01). Low levels of parasites were detected by DL-based analysis on day three following treatment initiation, but a small number of fluorescent signals were detected also in microscopy-negative samples.
CONCLUSION
Quantification of P. falciparum parasites in DAPI-stained thin smears is feasible using DL-supported, point-of-care digital microscopy, with a high correlation to visual assessment of samples. Fluorescent signals from artefacts in samples with low infection levels represented the main challenge for the digital analysis, thus highlighting the importance of minimizing sample contaminations. The proposed method could support malaria diagnostics and monitoring of treatment response through automated quantification of parasitaemia and is likely to be applicable also for diagnostics of other Plasmodium species and other infectious diseases.

Identifiants

pubmed: 33201905
doi: 10.1371/journal.pone.0242355
pii: PONE-D-20-25154
pmc: PMC7671488
doi:

Substances chimiques

Azure Stains 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0242355

Déclaration de conflit d'intérêts

Johan Lundin and Mikael Lundin are founders and co-owners of Aiforia Technologies Oy, Helsinki, Finland. The Nvidia Corporation donated a GPU via the Academic Grant Application Program, which was used during this study. The prototype instrument used for digitization of the samples is developed and patented (patent number: US20180246306) by the University of Helsinki (Helsinki, Finland). This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Oscar Holmström (O)

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.

Sebastian Stenman (S)

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.

Antti Suutala (A)

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.

Hannu Moilanen (H)

Center of Microscopy and Nanotechnology, University of Oulu, Oulu, Finland.

Hakan Kücükel (H)

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.

Billy Ngasala (B)

Department of Women's and Children's Health, International Maternal and Child Health (IMCH), Uppsala University, Uppsala, Sweden.
Department of Medical Entomology and Parasitology, School of Public Health, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Andreas Mårtensson (A)

Department of Women's and Children's Health, International Maternal and Child Health (IMCH), Uppsala University, Uppsala, Sweden.

Lwidiko Mhamilawa (L)

Department of Women's and Children's Health, International Maternal and Child Health (IMCH), Uppsala University, Uppsala, Sweden.
Department of Medical Entomology and Parasitology, School of Public Health, Muhimbili University of Health and Allied Sciences, Dar es Salaam, Tanzania.

Berit Aydin-Schmidt (B)

Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.

Mikael Lundin (M)

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.

Vinod Diwan (V)

Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.

Nina Linder (N)

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Department of Women's and Children's Health, International Maternal and Child Health (IMCH), Uppsala University, Uppsala, Sweden.

Johan Lundin (J)

Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Department of Global Public Health, Karolinska Institutet, Stockholm, Sweden.

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